Canonical Allele Identifier: PA339480
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 216153

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ala697Val
CA030702
NM_001127510.3:c.2090C>T